Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/136937
Title: Enhanced anaerobic phenol degradation by conductive materials via EPS and microbial community alteration
Authors: Yan, Wangwang
Sun, Faqian
Liu, Jianbo
Zhou, Yan
Keywords: Engineering::Environmental engineering
Issue Date: 2018
Source: Yan, W., Sun, F., Liu, J., & Zhou, Y. (2018). Enhanced anaerobic phenol degradation by conductive materials via EPS and microbial community alteration. Chemical Engineering Journal, 352, 1-9. doi:10.1016/j.cej.2018.06.187
Journal: Chemical Engineering Journal
Abstract: Anaerobic biodegradation is a promising and economical process to remove phenol in the wastewater, although the reaction kinetics are often limited by the toxicity of phenol. This study proposed a strategy to accelerate phenol degradation and mitigate its inhibition on the bioprocess by adding conductive materials (CMs) into the anaerobic degradation system. The results showed that CMs could stimulate phenol degradation up to one–fold higher than that in control group. Certain extracellular polymeric substances (EPS) compounds that can act as electron shuttles, i.e. protein and humic substances, were greatly enriched with the existence of CMs. In particular, compared with control group, CMs supplemented groups had 2.3 and 10 to 20 folds low molecular weight protein in bound and soluble EPS, respectively. Carbon nanotube supplemented group exhibited 3 times higher humic substance in soluble EPS. The overall electron transport system activity in CMs groups was much higher than that in control groups. The addition of CMs enriched phenol degradation bacteria–Syntrophorhabdus, Brooklawnia, Treponema and Syntrophus, as well as electroactive methanogens–Methanosaeta. It is proposed that Syntrophus and Methanosaeta were the functional genera in methanogenic phenol degradation via extracellular electron transfer. This study revealed that the presence of CMs altered the EPS composition and microbial community of the system and made it become more favorable for extracellular electron transfer.
URI: https://hdl.handle.net/10356/136937
ISSN: 1385-8947
DOI: 10.1016/j.cej.2018.06.187
Rights: © 2018 Elsevier B.V. All rights reserved. This paper was published in Chemical Engineering Journal and is made available with permission of Elsevier B.V.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:CEE Journal Articles

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